Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026952403

FEI Number

3026952403

Entity Name

NUPRODX, INC.

City/State/Country

Madera, CA, US

Establishment Address

40380 Brickyard Drive, Suite 102, Madera, CA 93636, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Nuprodx, Inc. (Owner Number: 9042319)

Owner / Operator Contact Address

40380 Brickyard Drive; Suite 102, --, Madera, CA 93636, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

multichair

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
INB	Attachment, Commode, Wheelchair	Physical Medicine	Class 1	890.3920	2000-07-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nuprodx, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026952403. Last updated year: 2026. Please use registration number 3026952403 when referencing this establishment in official correspondence.